Phosphomolybdate@poly(diallyldimethylammonium chloride)-reduced graphene oxide modified electrode for highly efficient electrocatalytic reduction of bromate

被引:34
|
作者
Ding, Liang [1 ,2 ]
Liu, Yuping [1 ]
Guo, Si-Xuan [1 ]
Zhai, Jianping [2 ]
Bond, Alan M. [1 ]
Zhang, Jie [1 ]
机构
[1] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[2] Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210093, Jiangsu, Peoples R China
基金
澳大利亚研究理事会;
关键词
Polyoxometalates; Graphene; Poly(diallyldimethylammonium chloride); Bromate; Electrocatalysis; ROTATING-DISK ELECTRODE; WALLED CARBON NANOTUBES; FUNCTIONALIZED GRAPHENE; COMPOSITE FILM; ELECTROCHEMICAL PROPERTIES; PHOSPHOMOLYBDIC ACID; SILICOTUNGSTIC ACID; GOLD NANOPARTICLES; SINGLE-CRYSTALS; AQUEOUS-MEDIA;
D O I
10.1016/j.jelechem.2014.06.001
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Phosphomolybdate ([PMo12O40](3-) or PMo12) was adsorbed onto a poly(diallyldimethylammonium chloride) functionalized reduced graphene oxide (rGO-PDDA) modified glassy carbon electrode (GCE). Compared to monolayer formation of PMo12 on a bare GCE; the rGO-PDDA electrode has a significantly increased loading of PMO12, due to its much larger surface area. The presence of positively charged PDDA also favors the adsorption of negatively charged PMO12 and enhances the stability of the modified electrode. The fabricated electrode (PMo12@rGO-PDDA/GCE) was characterized by scanning electron microscopy as well as energy dispersive X-ray, Raman and FT-IR spectroscopies and applied to the electrocatalytic reduction of bromate. Cyclic voltammetry showed that PMo12@rGO-PDDA/GCE exhibits high electrocatalytic performance and good stability for the reduction of bromate. A wide linear current vs. bromate concentration response (0.02-10 mM) was achieved with excellent sensitivity (454 mu A cm(-2) mM(-1)). The kinetics for the electrocatalytic reduction of bromate and the number of electron involved were evaluated using the rotating disk electrode method. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 77
页数:9
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